Arthrex® AR-13710-12.5Recalls & reported problems
Arthrex, Inc. · CONTURLK HTO PLT,STRT WEDG 12.5MM LFT · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867014800), received between Jun 14, 2018 and Jun 14, 2018 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 14, 2018Break
IT WAS REPORTED THAT THE COMPLAINT IS RELATING TO A RING OF A CONTOUR H2O PLATE. THIS HAS MEAN´T THAT THERE WERE TWO REMAINING SCREWS, WHICH HAVE FAILED, AND THE PATIENT IS FACING A REVISION OSTEOTOMY. NO FURTHER INFORMATIONS AVAILABLE AT THE MOMENT. FOLLOW-UP INVESTIGATION: SCREW BROKE THROUGH RING IN PLATE. INITIAL SURGERY TOOK PLACE ON THE (B)(6) 2017. THE PERFORMED PROCEDURE AS A LEFT COMPLEX BIPLANE OPENING WEDGE OSTEOTOMY. THE REVISION OSTEOTOMY LEFT TIBIA SURGERY TOOK PLACE ON THE (B)(6) 2017 WHICH WAS COMPLETED SUCCESSFULLY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 7601492 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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